Cite
MLA Citation
Peter Gee et al.. “Cellular Reprogramming, Genome Editing, and Alternative CRISPR Cas9 Technologies for Precise Gene Therapy of Duchenne Muscular Dystrophy.” Stem cells international, vol. 2017, 2017, p. . http://access.bl.uk/ark:/81055/vdc_100082269553.0x000032